A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1046646



Internal ID19135865
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:110187239..110240591hg38UCSC Ensembl
Innerchr12:110625044..110678396hg19UCSC Ensembl
Innerchr12:109109427..109162779hg18UCSC Ensembl
Cytoband12q24.11
Allele length
AssemblyAllele length
hg3853353
hg1953353
hg1853353
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3524902
Samples
Known GenesIFT81
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1046646
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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